Vitafol One is a Oral Capsule, Gelatin Coated in the Human Prescription Drug category. It is labeled and distributed by Everett Laboratories, Inc.. The primary component is Vitamin A; Ascorbic Acid; Thiamine Mononitrate; Riboflavin; Niacin; Pyridoxine Hydrochloride; Cyanocobalamin; Folic Acid; Iodine; Magnesium; Zinc; Copper; Vitamin D; Omega-3 Fatty Acids; .alpha.-tocopherol; Iron.
Product ID | 0642-0070_50262876-4ef2-4eda-9b5e-f586a8bb7ce4 |
NDC | 0642-0070 |
Product Type | Human Prescription Drug |
Proprietary Name | Vitafol One |
Generic Name | Prenatal Supplement With Dha |
Dosage Form | Capsule, Gelatin Coated |
Route of Administration | ORAL |
Marketing Start Date | 2011-06-13 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Everett Laboratories, Inc. |
Substance Name | VITAMIN A; ASCORBIC ACID; THIAMINE MONONITRATE; RIBOFLAVIN; NIACIN; PYRIDOXINE HYDROCHLORIDE; CYANOCOBALAMIN; FOLIC ACID; IODINE; MAGNESIUM; ZINC; COPPER; VITAMIN D; OMEGA-3 FATTY ACIDS; .ALPHA.-TOCOPHEROL; IRON |
Active Ingredient Strength | 330 ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1 |
Pharm Classes | Vitamin A [CS],Vitamin A [EPC],Vitamin C [EPC],Ascorbic Acid [CS],Nicotinic Acid [EPC],Nicotinic Acids [CS],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [CS],Vitamin B12 [EPC],Copper [CS],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE],Vitamin D [CS],Vitamin D [EPC],Fatty Acids, Omega-3 [CS],Omega-3 Fatty Acid [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2011-06-13 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-06-13 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-06-13 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
VITAMIN A | 1100 [iU]/1 |
SPL SET ID: | 42a5cafd-a2c0-4ac2-99c9-708642f00716 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VITAFOL 88294273 not registered Live/Pending |
EXELTIS USA INC. 2019-02-08 |
VITAFOL 86653118 4859841 Live/Registered |
Exeltis USA, Inc. 2015-06-05 |
VITAFOL 73611865 1452861 Live/Registered |
EVERETT LABORATORIES, INC. 1986-07-28 |
VITAFOL 72084824 0728602 Live/Registered |
VITA ZAHNFABRIK H. RAUTER, KG 1959-11-06 |